Division of Pediatric Critical Care Medicine, Department of Pediatrics, OSF Children's Hospital of Illinois, Peoria, Illinois, USA.
Department of Pediatrics, Texas Center for Pediatric and Congenital Heart Disease, UT Health Austin/Dell Children's Medical Center, University of Texas Dell Medical School, Austin, Texas, USA.
J Interferon Cytokine Res. 2022 Jul;42(7):343-348. doi: 10.1089/jir.2022.0040. Epub 2022 Jun 15.
The impact of noninvasive ventilation (NIV) on local and systemic inflammation is poorly characterized, particularly when compared with invasive mechanical ventilation (IMV). We sought to quantify the local and systemic inflammatory response of these 2 respiratory treatments in rats with lipopolysaccharide (LPS)-induced lung injury (LPS-injured) and healthy rats. Animals were subjected to 4 h of NIV or IMV treatments at noninjurious settings, or 4 h of control treatment in which healthy or LPS-injured animals remained spontaneously breathing under isoflurane anesthesia with no respiratory support. Cytokines were then quantified in the serum and lung tissue by multiplex enzyme-linked immunosorbent assay. Contrary to our hypothesis, there were no significant differences in cytokine levels in serum or lung when comparing the NIV- and IMV-treated groups; this was true in both LPS-injured and healthy rats. However, within the LPS-injured group, pulmonary levels of interleukin (IL)-1α, IL-6, and tumor necrosis factor α were significantly lower in the NIV-treated group than in control but not in the IMV-treated group compared with control. We conclude that NIV, unlike IMV, could attenuate local inflammation.
无创通气(NIV)对局部和全身炎症的影响尚未得到充分描述,特别是与有创机械通气(IMV)相比时。我们试图通过脂多糖(LPS)诱导的肺损伤(LPS 损伤)大鼠和健康大鼠来量化这 2 种呼吸治疗的局部和全身炎症反应。动物在非损伤设置下接受 4 小时的 NIV 或 IMV 治疗,或在无呼吸支持的情况下,健康或 LPS 损伤的动物在异氟烷麻醉下自主呼吸 4 小时,接受对照治疗。然后通过多重酶联免疫吸附试验定量血清和肺组织中的细胞因子。与我们的假设相反,在比较 NIV 和 IMV 治疗组时,血清和肺中的细胞因子水平没有显着差异;在 LPS 损伤和健康大鼠中均如此。然而,在 LPS 损伤组中,与对照组相比,NIV 治疗组肺组织中的白细胞介素(IL)-1α、IL-6 和肿瘤坏死因子-α水平显着降低,但在 IMV 治疗组与对照组相比则没有降低。我们得出结论,NIV 与 IMV 不同,可减轻局部炎症。